R&D-driven manufacturing delivered globally
Scaling complex biosimilar development through deep chemical expertise, integrated software, and high-precision manufacturing capacity.
How we can help you
We provide comprehensive end-to-end solutions for biosimilar development, from analytical characterization to process optimization and regulatory support. Our services include:
Monoclonal Antibody (mAb) Biosimilars
End-to-End Bioprocess & Characterization
Regulatory Framework
Regulatory mAb guidelines · ICH Q5E (Comparability) · ICH Q6B · Quality Considerations · Totality-of-Evidence framework
- Vector design & transfection
- Stable clone selection
- Clone screening & productivity ranking
- Genetic stability assessment
- Cell banking (MCB/WCB support)
- Media optimization
- Feed strategy development
- DoE-based process optimization
- Scale-down models
- Perfusion modeling
- Protein A purification
- Ion exchange chromatography
- Hydrophobic interaction chromatography
- Ultrafiltration / Diafiltration
- Viral clearance model studies (collaborative)
- Intact mass analysis
- Peptide mapping
- Glycosylation profiling
- Charge variants (cIEF)
- Aggregation (SEC-MALS)
- Thermal stability (DSC)
- Binding affinity (SPR / BLI)
- ADCC / CDC assays
- Fc receptor binding
- Potency bioassays
- PK bioanalysis
- ADA assay development support
- Aggregation-related immunogenicity risk profiling
Peptide & Protein biosimilars
Analytical & Bioanalytical Services
Regulatory Framework
Regulatory Biosimilar Guidance (351(k)) · ICH Q6B · Scientific Considerations in Demonstrating Biosimilarity · Peptide sameness evaluation principles
- Primary structure confirmation
- Amino acid sequencing
- Mass accuracy determination
- Disulfide bond mapping
- Impurity profiling
- Circular Dichroism (CD) spectroscopy
- Fourier-Transform Infrared (FTIR) spectroscopy
- Nuclear Magnetic Resonance (NMR) spectroscopy
- X-ray crystallography support
- Thermal shift assays
- Receptor binding assays
- Cell-based potency assays
- Enzyme activity assays
- Immunogenicity risk assessment
- PK/PD studies
- Pre-formulation screening
- Excipient compatibility studies
- Forced degradation studies
- Accelerated stability studies
- Real-time stability studies
Meet Our Experts
Our team combines decades of experience in biosimilar development, regulatory strategy, and analytical characterization. We are committed to delivering high-quality, cost-effective solutions tailored to your needs.
Partner with Us for Your Biosimilar Development Needs
Whether you're developing a new biosimilar or optimizing an existing process, our team is ready to support you with world-class expertise and state-of-the-art facilities.
Get a Custom Quote
Fill out the form below, and our team will get back to you with a tailored proposal for your biosimilar development needs.